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Identification of a point mutation resulting in a heat-labile adenosine deaminase (ADA) in two unrelated children with partial ADA deficiency.
cDNA and amino acid sequence of human adenosine deaminase.
Identification of a point mutation in the adenosine deaminase gene responsible for immunodeficiency.
Long-term expression of human adenosine deaminase in mice transplanted with retrovirus-infected hematopoietic stem cells.
Long-term in vivo expression of a murine adenosine deaminase gene in rhesus monkey hematopoietic cells of multiple lineages after retroviral mediated gene transfer into CD34+ bone marrow cells.
Retrovirus-mediated gene transfer of human adenosine deaminase: expression of functional enzyme in murine hematopoietic stem cells in vivo.
Retrovirus-mediated transfer of human adenosine deaminase gene sequences into cells in culture and into murine hematopoietic cells in vivo.
Molecular genetics and potential gene therapy.
ADAR1 is essential for the maintenance of hematopoiesis and suppression of interferon signaling.
Human adenosine deaminase. cDNA and complete primary amino acid sequence.
Molecular cloning of human adenosine deaminase gene sequences.
Transient expression of human adenosine deaminase cDNAs: identification of a nonfunctional clone resulting from a single amino acid substitution.
Transfer and expression of human ADA in murine hematopoietic stem cells.
Expression defects of mutant human adenosine deaminase.
Adenosine-to-inosine RNA editing by ADAR1 is essential for normal murine erythropoiesis.